Canonical Allele Identifier: CA410734392

Gene: ZDHHC8

Linked Data

• gnomAD v4: 22-20139845-C-A
• MyVariant Identifiers: chr22:g.20127368C>A (hg19) ; chr22:g.20139845C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20139845C>A , CM000684.2:g.20139845C>A	GRCh38
NC_000022.10:g.20127368C>A , CM000684.1:g.20127368C>A	GRCh37
NC_000022.9:g.18507368C>A	NCBI36
NG_021420.1:g.13005C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334554.12:c.510C>A MANE Select	ENSP00000334490.7:p.Tyr170Ter
ENST00000320602.11:c.384+210C>A	ENSP00000317804.7:n.384+210C>A
ENST00000334554.11:c.510C>A	ENSP00000334490.7:p.Tyr170Ter
ENST00000405930.3:c.510C>A	ENSP00000384716.3:p.Tyr170Ter
ENST00000436518.5:c.477C>A	ENSP00000412807.1:p.Tyr159Ter
ENST00000468112.5:n.58-772C>A
NM_001185024.1:c.510C>A	NP_001171953.1:p.Tyr170Ter
NM_013373.3:c.510C>A	NP_037505.1:p.Tyr170Ter
XM_006724239.2:c.510C>A	XP_006724302.1:p.Tyr170Ter
NM_001185024.2:c.510C>A	NP_001171953.1:p.Tyr170Ter
NM_013373.4:c.510C>A MANE Select	NP_037505.1:p.Tyr170Ter